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Items: 1 to 20 of 120

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6913969copy number variation1nstd229human GRCh38 chr11: 46,386,983-46,387,139 , GRCh37.p13 chr11: 46,408,533-46,408,689 CHRM4
    nsv6910252copy number variation1nstd229human GRCh38 chr11: 46,359,860-46,749,716 , GRCh37.p13 chr11: 46,381,410-46,771,266 AMBRA1, ARHGAP1, 12 more genes
    nsv6903611copy number variation1nstd229human GRCh38 chr11: 46,391,401-46,403,768 , GRCh37.p13 chr11: 46,412,951-46,425,318 AMBRA1, CHRM4
    nsv6470528copy number variation1nstd223human GRCh38 chr11: 46,386,979-46,387,139 , GRCh37.p13 chr11: 46,408,529-46,408,689 CHRM4
    nsv6315537copy number variation1nstd102humanPathogenic GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576 PYGM, ATL3, 2125 more genes
    nsv6315474copy number variation1nstd102humanPathogenic GRCh37 chr11: 43,607,886-61,466,671 , GRCh38.p12 chr11: 43,586,336-61,699,199 TRR-TCT3-2, OR4A41P, 494 more genes
    nsv6313964copy number variation1nstd102humanUncertain significance GRCh37 chr11: 46,248,477-46,748,132 , GRCh38.p12 chr11: 46,226,926-46,726,582 ARHGAP1, F2, 13 more genes
    nsv6309197copy number variation1nstd102humanUncertain significance GRCh37 chr11: 46,318,032-46,761,066 , GRCh38.p12 chr11: 46,296,481-46,739,516 MIR3160-2, RPS10P19, 12 more genes
    nsv6302127copy number variation1nstd186human GRCh37 chr11: 46,381,458-46,433,255 , GRCh38.p12 chr11: 46,359,908-46,411,705 CHRM4, MDK, 3 more genes
    nsv6291196copy number variation1nstd102humanPathogenic GRCh37 chr11: 40,117,145-46,920,718 , GRCh38.p12 chr11: 40,095,595-46,899,167 LINC02687, ALKBH3, 86 more genes
    nsv6132265copy number variation1nstd213human GRCh37 chr11: 46,130,000-46,900,001 , GRCh38.p12 chr11: 46,108,449-46,878,450 ARHGAP1, CHRM4, 23 more genes
    nsv6132108copy number variation1nstd213human GRCh37 chr11: 46,130,000-46,920,001 , GRCh38.p12 chr11: 46,108,449-46,898,450 ARHGAP1, CHRM4, 23 more genes
    nsv6032957copy number variation1nstd212human GRCh38 chr11: 46,386,979-46,387,139 , GRCh37.p13 chr11: 46,408,529-46,408,689 CHRM4
    nsv5927227copy number variation1nstd209human GRCh38 chr11: 46,386,979-46,387,138 , GRCh37.p13 chr11: 46,408,529-46,408,688 CHRM4
    nsv5563185sequence alteration1nstd206human GRCh38 chr11: 46,388,537-46,391,007 , GRCh37.p13 chr11: 46,410,087-46,412,557 CHRM4
    nsv5508401copy number variation1nstd206human GRCh38 chr11: 46,386,983-46,387,139 , GRCh37.p13 chr11: 46,408,533-46,408,689 CHRM4
    nsv5507746copy number variation1nstd206human GRCh38 chr11: 46,359,908-46,411,705 , GRCh37.p13 chr11: 46,381,458-46,433,255 MIR4688, MDK, 3 more genes
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv5380725copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr11: 45,827,353-47,804,770 , GRCh38.p12 chr11: 45,805,802-47,783,218 MIR4688, LOC112268075, 58 more genes
    nsv5355058translocation1nstd200human GRCh38 chr11: 46,386,983-46,386,983 , GRCh38 chr11: 46,387,139-46,387,139 , GRCh37.p13 chr11: 46,408,689-46,408,689 , GRCh37.p13 chr11: 46,408,533-46,408,533 CHRM4
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